跳至主要内容
临床试验/ACTRN12626000856314
ACTRN12626000856314进行中(未招募)不适用

Feasibility of a patient-held difficult intravenous access card: a pilot randomised controlled trial with embedded qualitative interviews.

Edith Cowan University0 个研究点目标入组 250 人开始时间: 2026年11月2日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
250

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 No limit(—)
性别
All

入选标准

  • Adults aged 18 years or older who are receiving care at Sir Charles Gairdner Hospital and are identified as having difficult intravenous access by a vascular access clinician or emergency department clinician. Difficult intravenous access may be identified by patient-reported history of difficult cannulation, previous documentation of difficult intravenous access, poor vein visibility or palpability, two or more failed peripheral intravenous cannulation attempts, requirement for ultrasound-guided cannulation, or referral/escalation to a vascular access clinician or more experienced inserter. Participants must be able to provide informed consent and complete electronic enrolment and follow-up procedures, either independently or with assistance where appropriate

排除标准

  • Patient in critical/emergency situation (such as CODE BLUE), immediate life-threatening situation, palliative care not requiring IV procedures or other similar clinical scenario and requiring vascular access*1b. This scenario is left to the discretion of the VAT or ED staff member, and they can determine whether recruitment is appropriate or not.
  • *1b Emergency Department: Adults classified by Australasian Triage Scale and determined as Category 1 or 2
  • Patient requiring primary vascular access, that is not peripheral IV (such as PICC line or port).
  • Paediatric patients (<18 years old).

研究者

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